Nerve Conduction Studies and Electromyography for Beginners to understand basic procedure and interpretations.
It can be used as a basic guideline and advance interpretation can be easily understood after you read it.
2. Objective
To familiarize Nerve Conduction Studies & Needle Electromyography as
diagnostic tools and interpret its findings
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3. Contents
1. Background
2. Basic Instrumentations
3. Sensory and Motor Nerve Conduction Studies
4. Late responses
5. Electromyography
6. Clinical Interpretations
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4. Electrodiagnosis
• Electrodiagnosis is the field of study that uses electrical technology to
study human neurophysiology. (Adam et al, 2020)
Types
• Conventional Electrodiagnostic Test
• Modern Diagnostic Tests
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5. Conventional Electrodiagnostic Test
Strength Duration Curve
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Rheobase Test
Chronaxie Test
Faradic/Galvanic Test
Reaction of Degeneration Test
Pulse Ratio
Accommodation
Galvanic Tetanus Ratio
13. Display System
1. Video Computer screen
2. Audio System
Sweep speed: Horizontal screen=
milliseconds
Sensitivity: vertical axis= response
amplitude
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14. Nerve Condition Studies
Test used to measure the speed of the electrical activity of a nerve
Nerve conduction studies can test sensory or motor nerve fibers and can
determine both the speed of conduction as well as the amplitude of the
electrical signal evoked following stimulation of a nerve. (Julie K et al, 2016)
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16. Nerve Condition Studies
Advantage
1. Differentiate Axonal loss from demyelination
2. Localizes the site of injury
3. Can assess severity of nerve lesion
4. Can distinguish the type of nerve lesion
5. Non invasive technique
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Jay M Weiss, Lyn D Weiss. Easy EMG. Boston (USA): Elsevier; 2016.
17. Nerve Condition Studies
Limitations
1. Routine studies primarily evaluate distal nerves
2. Very Mild axon loss without demyelination may not be detected.
3. Some deeper nerve branches cannot be easily tested.
4. It does not evaluate small fibers
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Jun Kimura. Electrodiagnosis in Nerve and Muscles fourth edition. Kyoto (JAP): oxford; 2012.
18. Nerve Condition Studies
Patient Preparation:
Informed Consent
Examine skin
Relaxed comfortable position
True Nerve length
Maintain skin temperature
Clean the skin with alcohol swab
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21. Sensory Nerve Condition Studies
Basic Principle of Nerve Stimulation
1. Sensory nerve is stimulated at one point where as Motor nerve is stimulated at
least 2 points along its course
2. Supramaximal stimulation is applied for Sensory Nerve Action Potential (SNAP)
and Compound Motor Action Potential (CMAP)
3. Cathode pole of electrode (Black) should be placed near to the active electrode
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Jun Kimura. Electrodiagnosis in Nerve and Muscles fourth edition. Kyoto (JAP): oxford; 2012.
22. Sensory Nerve Condition Studies
Electrode Placement : Sensory NCV
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Electrode Site
Active (Recording) Over the nerve
Reference 3-4 cm apart from
Active electrode
Stimulating
electrode
Along the course
of nerve to be
stimulated
Ground Between Active
and stimulating
Electrode
23. Motor Nerve Condition Studies
Electrode Placement: Motor NCV
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Electrode Site
Active
(Recording)
Over the muscle belly (motor
point)
Reference (E2
or G2)
Nearby Tendon or bone away
from the muscle
Stimulating
electrode
Along the course of nerve to
be stimulated
Ground Between Active and
stimulating Electrode
25. Nerve Condition Studies
1. Latency:
Time taken electrical impulse to travel from the
stimulation site to the recording site
Sensory Nerve: Depends upon the speed of
conduction of the fastest fiber and distance
between stimulus to active electrodes
Motor Nerve: Depends upon the speed of
conduction of the fastest fiber , distance
between stimulus to active electrodes,
neuromuscular transmission time and
propagation time along the muscle membrane.
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26. Nerve Condition Studies
2. Duration :
Measured from initial
negative peak to return to
baseline
Suggest the number of
nerve fiber
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27. Nerve Condition Studies
3. Amplitude:
Measured from baseline to
negative peak or negative
peak to positive peak
Suggest the density of nerve
fiber in Sensory NCS and
number of motor units in
Motor NCS.
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28. Nerve Condition Studies
4. Nerve Conduction Velocity (NCV):
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Distance between Active and stimulating electrode
onset latency
SNCV =
Distance between proximal and distal Stimulating site
Proximal latency- distal latency
MNCV =
29. Normative value :Amplitude
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Sensory
NCV
Nerve Amplitude
(micro Volt)
Nerve Amplitude
(micro Volt)
Median (S) >20.0 Sural (S) >10.0
Ulnar (S) >18.0 Lat Femoral
Cutaneous
10-25
Radial (S) >10.0 Superficial
fibular (S)
10-26
Motor NCV
Nerve Amplitude
(m Volt)
Nerve Amplitude
(m Volt)
Median (M) >4.0 Fibular >2.0
Ulnar (M) >4.0 Medial Plantar >3.0
Radial (M) >3.0 Lateral plantar >3.0
30. Normative Value :NCV
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Sensory CV
Nerve Velocity (m/s) Nerve Velocity (m/s)
Median (S) >45.0 Sural (S) >36.0
Ulnar (S) >45.0 Lat Femoral
Cutaneous
> 44
Radial (S) >44.0 Superficial
fibular (S)
45.5-56.9
Motor CV
Nerve Velocity (m/s) Nerve Velocity (m/s)
Median (M) >50.0 Fibular >40.0
Ulnar (M) >50.0 Medial Plantar > 40.0
Radial (M) >50.0 Lateral plantar >40.0
31. Normative Value :Distal Latency
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Sensory CV
Nerve Latency (ms) Nerve Latency (ms)
Median (S) <1.9 Sural (S) <3.8
Ulnar (S) <3.1 Lat Femoral
Cutaneous
<2.6
Radial (S) <3.4 Superficial
fibular (S)
<2.4
Motor CV
Nerve Velocity (m/s) Nerve Velocity (m/s)
Median (M) <4.2 Fibular <5.5
Ulnar (M) <3.4 Medial Plantar <6.0
Radial (M) <2.9 Lateral plantar <6.0
32. To Memorize
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Nerve Upper limb Lower Limb
Latency <4.0 ms <6.0 ms
Sensory Amplitude >10.0 µV >10.0 µV
Motor Amplitude >4.0 mV >3.0 mV
NCV 40-50 m/s 35-45 m/s
33. H Reflex
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Monosynaptic reflex
Assess proximal lesions
Submaximal stimulation
Involves sensory and motor neurons
Reflex arch of H Reflex:
• Ia sensory fiber
• Spinal cord and its interneuron
• Efferent motor fiber
Supramaximal stimulation: No H-
reflex
34. H Reflex
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Normal value in Soleus H
reflex in adults
• Latency (ms): 30.3 ± 1.7
• Amplitude (mV): 9.8 ± 6.1
• M-wave (mV): 24.6 ±6.6
• HM ratio: 0.4 ± 0.2
Clinical Implications
• Evaluates proximal sensory & motor
pathways
• GBS: absent, delayed or dispersed
• S1 radiculopathy: delayed or absent
35. F Wave
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Supramaximal stimulation
No reflex arch
Evaluates
Root or plexus abnormalities
Neuropathy
myopathy
Helpful in diagnosis of
GBS
Thoracic outlet syndrome
Brachial plexus injury
Radiculopathies with more than
one root involved
39. Diabetic neuropathy
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DISTAL LATENCY
CMAP AMPLITUDE
SNAP AMPLITUDE
NORMAL OR
NEAR NORMAL
REDUCTION
REDUCTION
40. Radiculopathy
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CMAP AMPLITUDE
F WAVE
H REFLEX REDUCED/ABSENT
REDUCTION
REDUCED/ABSENT
41. Pronater teres syndrome
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PROXIMAL LATENCY AT
FOREARM
DISTAL LATENCY AT
WRIST
CMAP AMPLITUDE
FOREARM
WRIST
PROLONGED
NORMAL
NORMAL
42. Variables affecting NCV Studies
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Physiological Variables Technical variables
Age Stimulating system
Temperature Recording System
Upper limb vs Lower limb Inadvertent stimulation of
another nerve
Gender Anomalous innervation of
muscles
43. Electromyography (EMG)
• Recording of action potential of muscle fibers firing singly or in a group, near the
needle electrode in a muscles (Mishra & Kalita, 2014)
• EMG test the integrity of entire motor system, which consists of upper and lower
motor neurons, neuromuscular junction and muscles (Kimura, 2016)
• Performed as an extension of physical examination rather than laboratory
procedure.
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47. EMG Procedure
• Preparation of patient
• Select the muscles to be tested
• Locate the site of needle insertion
• Insert the needle quickly
• Sharp Motor Unit Potential (MUP) on minimal voluntary contraction
confirms that needle is in proper position. If MUP is not sharp,
reposition the needle
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48. Neuropathy vs Myopathy
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Neuropathy Myopathy
Number of motor neuron decreases Muscle fibers are destroyed
Deprived muscles fibers get collateral from
viable motor neuron
Decreased number of muscle fibers
supplied by a single motor neuron
Increased number of muscle fibers supplied
by a single motor neuron
Decrease in size of motor unit
Amplitude and duration of Motor unit action
potential increases
Amplitude and duration of Motor unit
action potential decreases
49. EMG Analysis
1. Insertional Activity
2. Muscles at Rest
3. Motor Unit Analysis on mild voluntary contraction
4. Maximum voluntary contraction
• Recruitment pattern
• Interference pattern
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52. Insertional activity
Insertional activity Seen in
Increased Early stage of denervation
Acute myositis
Inflammatory myopathies
Decreased Atrophied muscles
Fibrosed muscles
Needle electrode is not in
muscle tissue
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67. Motor Unit Action Potential (MUAP)
• Analysis of MUAP done with
minimal contraction of muscles
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68. Motor Unit Action Potential (MUAP)
Component Normative value
Amplitude 4 µV to 5 mV
Duration 2 ms to 17 ms
Rise time Upto 500 ms
Frequency 1 Hz- 60 Hz
Phase Mono to Four
phases
(Bi-phasic or Tri-
phasic)
Sound Clear, sharp
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70. Motor Unit Action Potential (MUAP)
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Amplitude and Duration
Increased in Neuropathy
Decreased in myopathy
71. Motor Unit Action Potential (MUAP)
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Phases
Normal triphasic
Polyphasic
+ Longer
Duration
Neurogenic abnormalities
+ Shorter Myopathic
72. Examination of Muscles at Maximum
Voluntary Contraction
• Change in electrical activity during progressively increasing
contraction to maximal contraction
1. Recruitment
2. Interference pattern
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73. Recruitment & Interference
• The motor unit start firing in a regular pattern at 5 Hz
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Normal
Neurogenic
Myopathic
77. EMG finding in DMD
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DECREASED/ ABSENT
Fibrillation Potential, Positive sharp waves
Low amplitude, Short duration, Polyphasic
Low amplitude and Reduced
Insertional Activity
Spontaneous
Activity
Motor Unit Potential
Interference
78. EMG finding in Gullian Barre Syndrome
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Increased
Fasciculation or Myokymic
High amplitude, long duration, Polyphasic
High amplitude and Reduced
Insertional Activity
Spontaneous
Activity
Motor Unit Potential
Interference
79. Role of EMG and NCV Tests in Physiotherapy
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EVALUATE TREATMENT OUTCOME
NEUROMUSCULOSKELETAL ASSESSMENT
PLAN PHYSIOTHERAPY INTERVENTION
80. Take Home Message
1. NCV : demyelinating and axonal neuropathy
2. Late responses (F wave and H-reflex) : Radiculopathy and proximal neuropathy
3. Electromyography studies differentiates myopathy with neuropathy
4. All these tests are extensions of physical examinations
5. Findings of Electrodiagnosis tests can be valuable to plan physiotherapy
interventions based on severity and type of neuromusculoskeletal injuries
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Has two Electrodes:
Cathode/ Negative pole/Black
Anode/Positive/ Red
Cathode is placed towards the direction of stimulation (except F wave)
Supramaximal stimulation: 10-12%
Constant Current Stimulator and Constant Voltage Stimulator
Severity of lesion: neuropraxia, Axonotmesis and Neurotmesis
type of nerve lesion : sensory, motor or mixed
4: only fast fibers, myelinated fibers
Examine skin: for sensitivity and integrity
True Nerve length: For Ulnar nerve, flexed elbow
Maintain skin temperature: at 34 degree Celsius.
Motor NCV :The distance between two points should be at least 10 cm
Normal Supramaximal stimulation for MNCV: 20-50 mA, SNCV: 5-30 mA
Motor nerve is stimulated at least 2 points along its course : NMJ and muscle depolarizn time
Cathode pole of stimulating electrode should be placed close to the active electrode
: prevents hyperpolarization effect of anode and anodal conduction block
CMAP: summative AP of motor units, more amplitude (mV), longer duration
SNAP: summative AP of sensory N fibers, less amplitude (µV), shorter duration
Skin Temp : 32 degree Celsius UE, 30 degree for LE
Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
Skin Temp : 32 degree Celsius UE, 30 degree for LE
Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
Skin Temp : 32 degree Celsius UE, 30 degree for LE
Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
Skin Temp : 32 degree Celsius UE, 30 degree for LE, 8 cm distal stim site
Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
Skin Temp : 32 degree Celsius UE, 30 degree for LE, distal latency 8 CM
Side to side amplitude difference of >50 % or 20 % amplitude drop distal to proximal is significant
Electrodes: Active: Gastrosoleus, Reference: TA, Stimulating: Popliteal fossa (for S1 radiculopathy)
H reflex UE: Flexor carpi radialis, Median nerve at cubital fossa (C6-C7) radiculopathy
H reflex disappear when stimulation is further increased
Significance: Assess proximal lessions, becomes abnormal early in radiculopathy, assess preganglionic lesion
Before 2 years Seen in every muscles
Shorter conduction time of S1 due to less dispersion of Ia fiber of nerve
Obtained from any distal muscles
Depolarization of axon hillock—depolarization of dendrite—in turn depolarization of axon hillock
select portion of these alpha motor neurons, (roughly 5-10% of available motor neurons), 'backfire' or rebound
Only few (10%) of motor neuron particpitaes in F wave
Explores only the motor component of peripheral nerve
Small amplitude response occurring 20-60 ms after direct muscle response (m-wave)
Chronodispersion: diff bw minimum and max latencies in series (50-60) of F wave
F-M ratio: latencies of F wave: M wave
Persistence: no of response occurrence divided by no of stimuli
50-75 % decrease in CMAP amplitude: moderate axon loss
75%: severe axonal loss
Absent CMAP: no viable axon
Primarily Demyelinating Neuropathy
Proximal weakness
Mainly affecting motor nerves
Mainly axonal degeneration, distally
Neuropraxia
Compression of Median nerve at pronater teres, without conduction block
Age:
Infant has half NCV than adult: immature myelin sheet
After 60 yrs NCV decreases: degeneration of nerve
Temperature:
Decrease in temp=latency increases, NCV decreases and amplitude increases
Due to closure of ca channel
1 degree fall in temp incrases 0.3 ms latency
Increasing temp (29-38), NCV increases by 5 %
Idol skin temp : 34 degree
Upper limb Vs lower limb
Shorter UL nerve has longer internodal distance, large diameter of axon= increases NCV
Longer LL nerve have many branches and lower temp than UL
Male NCV<Female NCV (Fat increases core temp in female)
Surface EMG assesses muscle function by recording muscle activity from the surface above the muscle on the skin.
Surface EMG can be recorded by multiple electrodes.
Limitations: Recordings are restricted to superficial muscles
Uses: Kinesological Assessments, Research purpose and Biofeedback.
Morbid obesity: difficult to localize specific muscles
Thin individuals: not to insert needle deep to avoid injury to other tissues ( thoracis-lung)
Needle location: slightly away from motor point to avoid end plate noise
Insertional activity: caused by mechanical damage to muscles
Spontaneou activity: muscles at rest
Short burst of electrical activity (clusters of sharp positive and negative spike) lasts for < 300ms
Insertional activity: caused by mechanical damage to muscles causing depolarization
Sound: Crisp (wringing the paper)
Increased: electrical activity lasts longer than 300 ms, due to unstable or excitable muscle fiber membrane
Decreased: shorter
Inflammatory myopathies Polymyositis, dermatomyositis
Fibrosed muscles: muscular dystrophy diseases ( due to unsynhronous opening and closing of na-K channel)
Denervation: acetylcholineesterage inhibition
Miniature Endplate Potential (MEEP): spont release of ach , creates a small current
short duration, irregular, small amplitude (10-20 microvolt)
Endplate spike: large amount of ach release, produces short depolarizn
single muscle fiber depolarization, biphasic, initial negative defletion, 100-200 microvolt, 3-5 msec
Pain
Endplate region: activity seen when the needle is in endplate region
of a muscle fiber
Miniature Endplate Potential (MEEP): spont release of ach , creates a small current
short duration (1-2 ms), irregular, small amplitude (10-20 microvolt)
Endplate spike: large amount of ach release, produces short depolarizn
single muscle fiber depolarization, biphasic, initial negative defletion, 100-200 microvolt, 3-5 msec
Pain
PSW: small amplitude (20-100 µV) Mono or biphasic(primary +ve defln) , 0.5-15 Hz
Arises from spont depolarization of a single muscle fiber
Sound: dull thud; Appears earlier than Fibs after injury
LMNL: AHC ds, Radiculopathies, PNI, Polyneuropathies with axonal degeneration
Myopathies: Muscular dystrophies, polymyositis
Fibs: rate: small amplitude 10-300µV; biphasic (initial positive) @ 05-10 hz,
Arises from spont depolarization of a single muscle fiber
Sound: rain hitting a tin roof
LMNL: AHC ds, Radiculopathies, PNI, Polyneuropathies with axonal degeneration
Myopathies: Muscular dystrophies, polymyositis
PSW: dull thud; Appears earlier than Fibs after injury
FIBS: rain hitting roofs
CRD: local muscle arrhythmias, repetitive and regular firing of group of muscle fibers
appear and disappear suddenly
Suggests ongoing reinnervation
originated by the spont depolarization of a single fiber, followed by ephaptic spread (cell to cell)to an adjacent muscle fiber.
Frequency: 10-100 Hz, Amplitude: 50 microvolt-500 microvolt
Sound: motorboat
Usually seen in injury greater than 6 months (chronic neurogenic conditions and myopathies
CRD: local muscle arrhythmias, repetitive and regular firing of group of muscle fibers
Simple or complex spike pattern that appear suddenly and disappear
Suggests ongoing reinnervation
originated by the spont depolarization of a single fiber, followed by ephaptic spread (cell to cell)to an adjacent muscle fiber.
Frequency: 10-100 Hz, Amplitude: 50 microvolt-500 microvolt
Sound: motorboat
Usually seen in injury greater than 6 months (chronic neurogenic conditions and myopathies
myotonic:, waxing and waning appearance @ 20-100 hz
rate: 20-100 hz
Two forms of waves: psw morphology or Brief spikes pattern of biphasic or triphasic potentials
originated by the spont depolarization of a single fiber, followed by ephaptic spread (cell to cell)to an adjacent muscle fiber.
Sound: dive bomber
Seen in myotonic dystrophy, polymyositis, chronic radiculopathy
myotonic:
rate: 20-100 hz, waxing and waning appearance
Two forms of waves: psw morphology or Brief spikes pattern of biphasic or triphasic potentials
originated by the spont depolarization of a single fiber, followed by ephaptic spread (cell to cell)to an adjacent muscle fiber.
Sound: dive bomber (military aircraft)
Seen in myotonic dystrophy, polymyositis, chronic radiculopathy
Regular firing pattern and rhythms: 5-10 Hz
Due to hyperexcitability of peripheral nerve motor axons
Sound: soldier marching
Regular firing pattern and rhythms: 5-10 Hz
Due to hyperexcitability of peripheral nerve motor axons
Sound: soldier marching
Occurs randomly and irregularly @ 1 Hz-500 Hz
Signals Originate from spinal cord or peripheral nerve lesion causing contrctn of ms
Due to involuntary asynchronous contraction of bundles of ms fibers or a whole motor unit
Can occur in healthy individual or in diseases
Can be seen with naked eye
Sound: low pitched dump
Occurs randomly and irregularly @ 1 Hz-500 Hz
Signals Originate from spinal cord or peripheral nerve lesion causing contrctn of ms
Due to involuntary asynchronous contraction of bundles of ms fibers or a whole motor unit
Can occur in healthy individual or in diseases
Can be seen with naked eye
Sound: low pitched dump
Amplitude: measured from most positive to most negative peak; reflects muscle fiber density close to needle;
Rise Time: time lag from initial positive defletion to subsequent negative upward peak: Distance between needle and MU
Duration: initial departure from baseline to final return to baseline, Degree of synchrony between muscle fibers
Phases: peaks crossing baseline, Normal has 3 peaks, more than 4_ polyphasics
Clear, sharp Sound
Normal Polyphasic seen in : Upto 30 % in Monopolar & 15 % in concentric needle
AP of one muscle fiber: represents individual components of phase
Myopathic: reflects Regeneration of fibers & increase in fiber density in myopathies
Neuropathic: Regeneration of axons in neuropathies
Recruitment:
Interference
On voluntary contraction, smaller muscles fibers recruited first then larger: Henneman principle
Myokymia: Due to hyperexcitability of peripheral nerve motor axons
Neuromusculoskeletal assessment: type of lesion, severity
Active stage of disease: energy conservations technique
Recovery stage: gradual increase in treatment
Neuropraxia, Axonotmesis: